ENST00000347401.8:c.1299C>G
|
|
|
ENST00000353578.9:c.8036C>G
|
ENSP00000315873.4:p.Thr2679Ser
|
|
ENST00000682957.1:c.781C>G
|
|
|
ENST00000684508.1:n.921C>G
|
|
|
ENST00000295550.9:c.8654C>G
MANE Select
|
ENSP00000295550.4:p.Thr2885Ser
|
|
ENST00000295550.8:c.8654C>G
|
ENSP00000295550.4:p.Thr2885Ser
|
|
ENST00000347401.7:c.6830C>G
|
ENSP00000315609.4:p.Thr2277Ser
|
|
ENST00000353578.8:c.8036C>G
|
ENSP00000315873.4:p.Thr2679Ser
|
|
ENST00000409809.5:c.8036C>G
|
ENSP00000386844.1:p.Thr2679Ser
|
|
ENST00000472056.5:c.6833C>G
|
ENSP00000418285.1:p.Thr2278Ser
|
|
ENST00000491769.1:n.5096C>G
|
|
|
NM_004369.3:c.8654C>G , LRG_473t1:c.8654C>G
|
NP_004360.2:p.Thr2885Ser
|
|
NM_057166.4:c.6833C>G
|
NP_476507.3:p.Thr2278Ser
|
|
NM_057167.3:c.8036C>G
|
NP_476508.2:p.Thr2679Ser
|
|
XM_005246065.1:c.8054C>G
|
XP_005246122.1:p.Thr2685Ser
|
|
XM_005246066.1:c.7433C>G
|
XP_005246123.1:p.Thr2478Ser
|
|
XM_006712253.1:c.8153C>G
|
XP_006712316.1:p.Thr2718Ser
|
|
XM_011510574.1:c.8651C>G
|
XP_011508876.1:p.Thr2884Ser
|
|
XM_011510575.1:c.6248C>G
|
XP_011508877.1:p.Thr2083Ser
|
|
XM_017003304.1:c.6248C>G
|
XP_016858793.1:p.Thr2083Ser
|
|
XM_024452684.1:c.7433C>G
|
XP_024308452.1:p.Thr2478Ser
|
|
NM_004369.4:c.8654C>G
MANE Select
|
NP_004360.2:p.Thr2885Ser
|
|
NM_057166.5:c.6833C>G
|
NP_476507.3:p.Thr2278Ser
|
|
NM_057167.4:c.8036C>G
|
NP_476508.2:p.Thr2679Ser
|
|